Potassium Carbonate → 1-[2-benzoylthio-3-methoxybutanoyl]L-proline

HRID 1252829노트

반응식

HRID 1252829 반응식
[NH:1]1[CH2:8][CH2:7][CH2:6][C@H:2]1[C:3]([OH:5])=[O:4].Br[CH:10]([CH:14]([O:16][CH3:17])[CH3:15])[C:11](Cl)=[O:12].[C:18]([OH:26])(=[S:25])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.C(=O)([O-])[O-].[K+].[K+]>[OH-].[Na+]>[C:18]([S:25][CH:10]([CH:14]([O:16][CH3:17])[CH3:15])[C:11]([N:1]1[CH2:8][CH2:7][CH2:6][C@H:2]1[C:3]([OH:5])=[O:4])=[O:12])(=[O:26])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

참가 물질

6

실험 절차

To a solution of L-proline (5.75 g) in N sodium hydroxide (50 ml) chilled in an ice bath, 2N sodium hydroxide (25 ml) and 2-bromo-3-methoxybutyric acid chloride [obtained from 2-bromo-3-methoxybutyric acid [J. Am. Chem. Soc., 71, 1096, (1949)] and thionyl chloride] (10.7 g) are added, with vigorous stirring. After three hours, thiobenzoic acid (7.5 g) and potassium carbonate (4.8 g) are added and the mixture is stirred at room temperature overnight. The reaction mixture is acidified and extracted with ethyl acetate. The organic layer is concentrated to dryness and the residue is chromatographed on a column of silica gel with benzene-acetic acid to yield N-[2-benzoylthio-3-methoxybutanoyl]-L-proline.

후처리

  1. extractionextracted with ethyl acetate
  2. concentrationThe organic layer is concentrated to dryness
  3. customthe residue is chromatographed on a column of silica gel with benzene-acetic acid

출처 및 근거

ORD 기록
ord-387804414a1645e685a15f0cb260fcc1
출처 데이터셋
uspto-grants-1988_05
특허 번호
US04745124

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